US5527919A - Process for the preparation of 1-[(1,1'-biphenyl]-4-YL]-methyl-1H-imidazole-5-carboxylic acids - Google Patents

Process for the preparation of 1-[(1,1'-biphenyl]-4-YL]-methyl-1H-imidazole-5-carboxylic acids Download PDF

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US5527919A
US5527919A US08/177,153 US17715394A US5527919A US 5527919 A US5527919 A US 5527919A US 17715394 A US17715394 A US 17715394A US 5527919 A US5527919 A US 5527919A
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alkyl
carbon atoms
group
product
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Neerja Bhatnagar
Jean Buendia
Christine Griffoul
Holger Heitsch
Adalbert Wagner
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Aventis Pharma SA
Anika Therapeutics Inc
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Roussel Uclaf SA
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    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/58—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring nitrogen atoms
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    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/18—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms, not being part of nitro or nitroso groups
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    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C311/52—Y being a hetero atom
    • C07C311/54—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea
    • C07C311/57—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/58—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings having nitrogen atoms of the sulfonylurea groups bound to hydrogen atoms or to acyclic carbon atoms
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D—HETEROCYCLIC COMPOUNDS
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    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Definitions

  • R 1 is selected from the group consisting of alkyl, alkenyl, alkynyl and alkylthio of up to 10 carbon atoms and cycloalkyl of 3 to 7 carbon atoms, all optionally substituted
  • R 2 and R 3 are individually selected from the group consisting of:
  • alkyl alkenyl, alkoxy and optionally oxidized alkylthio of up to 6 carbon atoms optionally interrupted by at least one --O--, --S-- or nitrogen and optionally substituted,
  • R is hydrogen or optionally substituted alkyl or phenyl
  • m 1 is an integer from 0 to 4
  • m 2 is an integer from 0 to 2
  • X is selected from the group consisting of a single bond, --NH--, --NHCO--, --NH--COO--, --N ⁇ CH--N--R 13 and --NHCONH--
  • R 10 and R 13 are individually selected from the group consisting of hydrogen, alkyl and alkenyl of up to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, optionally substituted phenyl and benzyl, pyridyl, nitropyridyl, pyrimidyl, tetrazolyl, diazolyl, piperidinyl, alkylpiperidinyl, thiazolyl, alkylthiazolyl, tetrahydrofuranyl and methylte
  • --SO 2 --NH--SO 2 --R 14 --NH--SO 2 --R 14 , --NH--SO 2 --R 14 , --PO 3 R 14 , --NH--SO 2 --CF 3 and ##STR4## --(CH 2 ) m1 --SO 3 R 14 , --CO--NH--OR 14 , --CO--NH--NH--SO 2 --CF 3 , --CO--NH--SO 2 --R 14 , --CH 2 SO 2 NHCO--R 14 ,
  • R 13 has the definition above and R 14 and R 15 are individually selected from the group consisting of hydrogen, alkyl of 1 to 6 carbon atoms, optionally substituted cycloalkyl of 3 to 6 carbon atoms, and Y is oxygen or sulfur, all the alkyl, alkenyl, cycloalkyl, alkylthio, phenylthio, alkoxy, phenyl, benzyl being optionally substituted by at least one member of the group consisting of halogen, hydroxyl, nitro, alkyl, alkenyl and alkoxy of up to 4 carbon atoms, trifluoromethyl, cyano, amino, mono and dialkylamino, free, salified or esterified carboxy, haloalkyl, alkylthio, haloalkylthio, haloalkoxy, phenyl, pyridyl, benzyl, phenethyl, benzoyl
  • R' 1 has the meaning indicated above for R 1 in which the optional reactive functions are optionally protected and Hal is halogen to obtain a product of the formula ##STR9## in which R' 1 and R' 3 and R' 4 have the meanings above, subjecting the latter to an addition reaction on the CN with a reagent capable of introducing R' 2 having the meaning above for R 2 in which the optional reactive functions are optionally protected to obtain a product of the formula ##STR10## in which R' 1 , R' 2 , R' 3 and R' 4 have the meanings above, optionally subjecting the latter to a substitution reaction of the oxygen by a sulfur to obtain a product of the formula ##STR11## in which R' 1 , R' 2 , R' 3 and R' 4 have the meanings above, subjecting the product of formula E or the product of formula L to a cyclization reaction to obtain a product of the formula ##STR12## in which R' 1 , R' 2 , R' 3 and R' 4 have the meanings above,
  • --(CH 2 ) m1 --S(O) m2 --X--R 10 when m 1 is other than 0, --(CH 2 ) m1 -- is alkylene such as methylene, ethylene, n-propylene or n-butylene and preferably when m is 0, 1 or 2, --(CH 2 ) m1 -- is a single bond, methylene or ethylene.
  • --S(O) m2 --X--R 10 moiety may be in a non-exhaustive manner selected from the group consisting of:
  • the alkyl preferably designates methyl, ethyl, propyl, isopropyl, butyl isobutyl, sec.-butyl and tert-butyl but can also be pentyl or hexyl and particularly isopentyl and isohexyl.
  • alkenyl preferably designates vinyl, allyl, 1-propenyl, butenyl and particularly 1-butenyl or pentenyl.
  • alkynyl preferably designates ethynyl, propynyl and linear or branched butynyl.
  • alkyls interrupted by one or more heteroatoms there are methoxymethyl, methoxyethoxymethyl, propylthiopropyl, propyloxypropyl, propylthioethyl, methylthiomethyl.
  • Halogen preferably designates chlorine or bromine, but can also be fluorine or iodine.
  • alkoxy preferably designates methoxy, ethoxy, propoxy or isopropoxy, but can also be n- or secondary or tertiary butoxy.
  • the acyl preferably is derived from an organic carboxylic acid of 1 to 6 carbon atoms such as formyl, acetyl, propionyl, butyryl or benzoyl, but also pentanoyl, hexanoyl, acryloyl, crotonoyl or carbamoyl.
  • the amino substituted by one or two alkyls preferably designates groups in which the alkyl is chosen from the alkyls defined above such as for monoalkyl amino, methylamino or ethylamino, or for dialkylamino dimethylamino or methylethylamino.
  • Acyloxy designates an acyl with the values indicated above may be formyloxy, acetyloxy, propionyloxy, butyryloxy or benzoyloxy.
  • Cycloalkyl preferably designates cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
  • the monocyclic and condensed rings designate saturated or unsaturated rings.
  • saturated monocyclic are pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidyl, piperazinyl, morpholinyl, thio-morpholinyl, azepinyl, or unsaturated monocycles such as: pyrannyl, pyrrolyl, imidazolyl, pyrazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, thiazolyl, thiadiazolyl, oxazolyl, furazannyl, pyrrolinyl such as delta 2-pyrrolinyl, imidazolinyl such as delta 2-imidazolinyl, pyrazolinyl such as delta 3-pyrazolinyl as well as the position isomers of the heteratom or heteroatoms which these radicals can contain such as isothiazoly
  • the condensed rings may be saturated such as 1-oxa spiro [4,5]decyl, tetrahydropyran-2-spirocyclohexyl, cyclohexanespiro-2'-(tetrahydrofuran) or 1, 10-diaza anthr-4-yl, or unsaturated such as benzothienyl, naphtho[2,3-b]thienyl, idenyl, indolizinyl, isoindolyl, 3H-indolyl, indolyl, indazolyl, purinyl, quinolizinyl, benzopyrrolyl, benzimidazolyl, isoquinolyl, quinolyl, phthalazinyl, naphthyridinyl, quinoxalinyl, quinazolinyl, cinnolinyl, pteridinyl, carbazolyl, beta-carbolinyl, acridiny
  • Haloalkyl is the alkyl as defined above and is substituted by one or more halogens as defined above for example bromoethyl, trifluoromethyl, trifluoroethyl or pentafluoroethyl.
  • Alkylthio preferably is the alkyl as defined above, for example methylthio or ethylthio and haloalkylthio preferably is the alkyl as defined above, for example methylthio or ethylthio and haloalkylthio preferably is the alkyl as defined above and is substituted by one or more halogens as defined above, for exampled bromoethylthio, trifluoromethylthio, trifluoroethylthio or pentafluoroethylthio.
  • Haloalkoxy preferably is the alkoxy as defined above and is substituted by one or more halogens as defined above, for example bromoethoxy, trifluoromethoxy, trifluoroethoxy or pentafluoroethoxy.
  • Carbamoyl also designates carbamoyl substituted by a lower N-monoalkyl carbamoyl such as N-methylcarbamoyl, N-ethylcarbamoyl, a lower N,N-dialkyl carbamoyl such as N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl; and N-(lower hydroxyalkyl) carbamoyl such as N-(hydroxymethyl) carbamoyl, N- (hydroxyethyl) carbamoyl, a lower carbamoylalkyl such as carbamoylmethyl and carbamoylethyl.
  • Phenyl substituted by an alkylthio is for example benzylthio.
  • alkyl, alkenyl, cycloalkyl and phenyl which ca be represented by or carried by R 1 , R 2 and R 3 can take the valuses defined above and may or more note substituted by one or more identical or differnet substituents as defined above.
  • R 2 and R 3 can, for example, be alkylthio, phenylthio, alkylsulfine phenylsulfinyl, alkylsufonyl or arylsufonyl but also cycloalkylthio such as cyclohexylthio:
  • Alkylthio, alkylsulfuinyl and alkylsufonyl may be linear or branched alkyl as indicated above the the alkyl.
  • Examples are, methylthio, hydroxymethylthio, ethylthio, aminoethylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl, ethylsulfonyl, propylthio, isopropylthio, butylthio, sec-butylthio, ter-butylthio, isopentylthio or isohexylthio or those in which the thio is oxidized into the sulfinyl or sulfonyl.
  • R 2 and R 3 can also be phenylthio, pyridylthio or pyrimidylthio, imidazolylthio, N-methylimidazolylthio as well as those in which the thio is oxidized into the sulfinyl or sulfonyl such as phenylsulfinyl or phenylsulfonyl.
  • substituted alkyls there are those substituted by one or more phenyl for example, benzyl, diphenylmethyl and tripehnylmethyl, and those substituted by pyridyl, for example pyridylmethyl, it being understood that in the non-exhaustive list of examples as mentioned above, the alkyl can also just as equally be ethyl, propyl or butyl such as phenylethyl.
  • substituted alkenyl are those substituted with at least one phenyl or pyridyl, as indicated in the examples given above in which the alkyl is replaced by an alkenyl for example phenylvinyl or phenylallyl.
  • the carbamoyl and amino radicals mentioned above in particular: ##STR18## designate groups in which two identical or different groups are linked to the nitrogen atom selected from the group consisting of hydrogen to obtain the amino; the alkyl as defined above to obtain the monoalkyl- or dialkylamino in which the linear or branched alkyl have 1 to 6 carbon atoms and particularly methyl, ethyl, isopropyl, methoxymethyl, methoxyethyl, ethoxyethyl radicals; the phenyl, benzyl, phenethyl optionally substituted to obtain the phenylamino or benzylamino.
  • the substituted carbamoyl there are lower N-monoalkyl carbamoyl, for example, N-methylcarbamoyl, N-ethylcarbamoyl; the lower N,N-dialkyl carbamoyl, for example, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl; the N-(lower hydroxyalkyl) carbamoyl, for example, N-(hydroxymethyl) carbamoyl, N-(hydroxyethyl) carbamoyl; the lower carbamoylalkyl, for example carbamoylmethyl, carbamoylethyl; phenylcarbamoyl; pyridylcarbamoyl; benzylcarbamoyl; N-methyl N-phenylcarbamoyl; pyridylmethyl-carbamoyl.
  • N-monoalkyl carbamoyl for
  • amino acid preferably designates a remainder derived from one of the natural amino acids such as glycine, alanine, valine, leucine, isoleucine, phenylalanine and particularly proline or one of the other natural amino acids known to one skilled in the art.
  • --(CH 2 ) m1 --X--R 10 which can be represented by R 6 , R 7 , R 8 or R 9 are --NH--SO 2 --CH 3 , --NH--SO 2 --C 6 H 5 , --NH--SO 2 --CF 3 , --NH--CH 2 --SO 2 --NH--C 6 H 5 , --CO--NH--SO 2 --C 2 H 5 , --CO--NH--SO 2 --CH 3 , --CO--NH--SO 2 --CH 2 --C 6 H 5 .
  • the heterocycle which can be formed with R 6 and R 7 or R 8 and R 9 is preferably saturated.
  • the acyl of R 8 and R 9 can be chosen from acetyl, propionyl, butyryl, pentanoyl and carbamoyl.
  • R 8 or R 9 is alkoxy-carbonyl, this is preferably tert-butyloxycarbonyl.
  • the carboxy of the products of formula I can be salified or esterified by various groups known to one skilled in the art among which there can be mentioned, for example: among the salification compounds, mineral bases such as sodium, potassium, lithium, calcium, magnesium or ammonium salt or organic bases such as methylamine, propylamine, trimethylamine, diethylamine, triethylamine, N,N-dimethylthanolamine, tris (hydroxymethyl) amino methane, ethanolamine, pyridine, picoline, dicyclo-hexylamine, morpholine, benzylamine, procaine, lysine, arginine, histidine, N-methylglucamine.
  • mineral bases such as sodium, potassium, lithium, calcium, magnesium or ammonium salt or organic bases
  • organic bases such as methylamine, propylamine, trimethylamine, diethylamine, triethylamine, N,N-dimethylthanolamine, tris (hydroxymethyl) amino methane, ethanolamine
  • esterification compounds are alkyl to form alkoxy carbonyl groups such as methoxycarbonyl, ethoxycarbonyl, tertbutoxycarbonyl or benzyloxycarbonyl which alkyls may be substituted by members selected from the group consisting of halogen, hydroxyl, alkoxy, acyl, acyloxy, alkylthio, amino or aryl such as chloromethyl, hydroxypropyl, methoxymethyl, propionyloxymethyl, methylthiomethyl, dimethylaminoethyl, benzyl or phenethyl.
  • alkyl to form alkoxy carbonyl groups such as methoxycarbonyl, ethoxycarbonyl, tertbutoxycarbonyl or benzyloxycarbonyl
  • alkyls may be substituted by members selected from the group consisting of halogen, hydroxyl, alkoxy, acyl, acyloxy, alkylthio, amino or aryl such as
  • the addition salts with mineral or organic acids of the products of formula I can be the salts formed with the following acids: hydrochloric acid, hydrobromic acid, hydroiodic acid, nitric acid, sulfuric acid, phosphoric acid, propionic acid, acetic acid, formic acid, benzoic acid, maleic acid, fumaric acid, succinic acid, tartaric acid, citric acid, oxalic acid, glyoxylic acid, aspartic acid, ascorbic acid, alkylmonosulphonic acid such as methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, alkyldisulfonic acid such as methanedisulfonic acid, ⁇ , ⁇ -ethanedisulfonic, arylmonosulfonic such as benzenesulfonic acid and aryldisulfonic acid.
  • acids formic acid, benzoic acid, maleic acid, fumaric acid, succinic acid, tart
  • R 2 and R 3 both are individually an optionally oxidized sulfurous alkylthio or phenylthio
  • the preferred products of the invention are particularly the products of formula I in which these sulfurous groups have the same degree of oxidation.
  • R 2 and R 3 are those wherein one of R 2 and R 3 is an optionally oxidized sulfur group as defined above and the other is alkyl, alkoxy, free, salified or esterifed carboxy or optionally substituted phenyl, preferably R 2 is the sulfurous group.
  • R 2 and/or R 3 may be alkylthio or alkenylthio optinally substituted with at least one member of the group consisting of formyl, --OH, alkoxy, acyloxy, free, salified or esterified carboxy; amino; substituted amino; carbamoyl; substituted carbamoyl; alkylthio; phenylthio; pyridinyl; pyrimidinyl; phenyl.
  • R 2 and R 3 are amino and carbamoyl, particularly substituted by one or two alkyl and amino acids mentioned above.
  • the substituted amino and carbamoyl which can be carried by R 2 and R 3 can also form a heterocycle such as those mentioned above.
  • R 2 and R 3 can be alkylthio substituted by one or more halogens such as chlorine and fluorine such as --S--CF 3 ; --S--CHF 2 ; --S--CH 2 F; --S--CF 2 --CHF 2 ; --S--CF 2 --CHFCl.
  • halogens such as chlorine and fluorine such as --S--CF 3 ; --S--CHF 2 ; --S--CH 2 F; --S--CF 2 --CHF 2 ; --S--CF 2 --CHFCl.
  • R 2 and R 3 can represent the following in which n, n1 and n2, individually may be 0 to 2 such as ##STR19## --SO 3 H; --S--CH 3 ; --S--(CH 2 ) n1 --S--(CH 2 ) n2 --X 4 ;
  • X 4 is H, OH, cyclohexyl, pyridyl, phenyl, CHO, COOH, NH 2 or ##STR20##
  • R 2 and R 3 can be particularly, --COOH; --CO 2 X 5 ; --SX 5 ; --NH 2 ; --C.tbd.N; --OMe; --OEt; --C ⁇ CH--COOH; tetrazolyl; ##STR21## in all their isomer, cis-trans isomer forms, ##STR22## --NH--CH 2 --COO--X 5 --NH--COO---X 5
  • X 5 is alkyl or aryl.
  • R 2 and R 3 can preferably be ##STR23##
  • the products of formula I represent in particular products in which R 2 and R 3 have the meanings indicated above and quite particularly products in which R 2 is an optionally substituted alkylthio as defined above or an alkoxy such as methoxy and R 3 is a free, salified or esterified carboxy or an amidified carboxy such as --COOH, --COO-methyl, --COO-ethyl, --CONH 2 or ##STR24##
  • R 4 are cyano, --(CH 2 ) m1 --SO 2 --X--R 10 as defined above and more particularly
  • the invention is preferably the above process for the preparation of products of the formula ##STR26## in which: R 1a is alkyl or alkenyl of up to 4 carbon atoms,
  • R 2a and R 3a are individually chosen from:
  • R 6a , R 7a , R 8a and R 9a are individually chosen from hydrogen, amino acids, alkyl of 1 to 6 carbon atoms, phenyl, benzyl, phenethyl or R 6a and R 7a and R 8a and R 9a form respectively with the nitrogen atom to which they are linked a heterocyclic selected from the group consisting of imidazolyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, pyridyl, piperidinyl, pyrimidinyl, pyridazinyl, pyrazinyl, piperazinyl, phenylpiperazinyl, piperidyl, oxazolyl, morpholinyl and thiomorpholinyl, azepine, indolyl, optionally substituted by at least one member of the group consisting of halogen, hydroxyl, nitro, alkyl and alk
  • alkyl and alkenyl being optionally substituted by at least one member of the group consisting of halogen, hydroxyl, nitro, alkyl, alkenyl and alkoxy of up to 4 carbon atoms, trifluoro-methyl, cyano, amino, mono- and dialkylamino, free, salified or esterified, carboxy, phenyl and tetrazolyl;
  • the said products of formula I a being in all possible racemic, enantiomeric and diastereoisomeric isomer forms, as well as the addition salts with mineral and organic acids or with mineral and organic bases of the said products of formula I a , characterized in that for their preparation as defined above, products of formulae A, II, III and a reagent capable of introducing the R' 2 are used in which R' 1 , R' 2 , R' 3 and R' 4 have the values indicated above for R 1a , R 2a , R 3a and R 4a respectively in which the reactive functions are optionally protected.
  • R 1b is alkyl of up to 1 to 4 carbon atoms
  • R 3b is hydrogen, formyl, acyloxy, alkyl or alkoxy optionally substituted or carboxy free, salified or esterified by an alkyl
  • R 2b is optionally substituted phenylthio, phenylsulfonyl, phenylsulfinyl, alkylthio, alkylsulfonyl or alkylsulfinyl such as in all those represented by R 2b and R 3b , alkyl and alkoxy of 1 to 6 carbon atoms
  • the phenyl is optionally substituted by one or more groups chosen from halogen, hydroxyl, trifluoromethyl, acyloxy, free, salified or esterified carboxy, phenyl, pyridyl, tetrazolyl, alkyl and alkoxy
  • R 10b and R 13b are, individually selected from the group consisting of hydrogen, methyl, ethyl, propyl, vinyl, allyl, pyridyl, phenyl, benzyl, nitropyridyl, pyrimidyl, tetrazolyl, diazolyl, piperidinyl, alkylpiperidinyl, thiazolyl, alkyl-thiazolyl, tetrahydrofuranyl and methyltetrahydrofuranyl, the said products of formula I b being in all possible racemic, enantiomeric and diastereoisomeric isomer forms, as well as the addition salts with mineral and organic acids or with mineral and organic bases of said products of formula I b , characterized in that for their preparation as defined above, products of formulae A, II, III and a reagent capable of introducing R' 2 are used in which R' 1 , R'
  • a more particular subject of the invention is the process for the preparation of products of the formula ##STR29## in which: R 1d is alkyl of 1 to 4 carbon atoms, R 3d is selected from the group consisting of carboxy free, salified or esterified by alkyl of 1 to 4 carbon atoms, formyl, acyloxy, alkyl of 1 to 4 carbon atoms optionally substituted by hydroxyl, R 2d is selected from the group consisting of phenylthio, phenylsulfonyl, phenylsulfinyl, alkylthio, alkylsulfonyl or alkylsulfinyl in which the alkyl has 1 to 4 carbon atoms, and R 4d is --SO 2 --NH 2 , --SO 2 --NH--CO--O--R 10d , --SO 2 --N ⁇ CH--NR 13d , or --SO 2 --NH--CO--NH--R 10d in which R 10d and R
  • a particular subject of the invention is the process as defined above, characterized in that a product of formula A is used in which R' 4 is --SO 2 --NH 2 , --SO 2 --NH--CO--O--R 10d , --SO 2 --N ⁇ CH--NR 13d , or --SO 2 --NH--CO--NH--R 10d in which R 10d and R 13d , are individually chosen from hydrogen, methyl, ethyl, n-propyl and propenyl, in which the reactive functions are optionally protected, a product of formula II in which R' 3 is carboxy free salified or esterified by alkyl of 1 to 4 carbon atoms, formyl, acyloxy, or alkyl of 1 to 4 carbon atoms optionally substituted by a hydroxyl, a product of formula III in which R' 1 is alkyl of 1 to 4 carbon atoms, and a reagent capable of introducing R' 2 in which R' 2 represents phenylthio, phen
  • a more preferred subject of the invention is the process as defined above, in which the product of formula A is used in which R' 4 is ##STR30## a product of formula II is used in which R' 3 is free salified or esterified alkoxy carboxy, a product of formula III is used in which R' 1 is alkyl of 1 to 4 carbon atoms and a reagent capable of introducing R' 2 when R' 2 is alkylthio or phenylthio optionally oxidized in the form of the sulfoxide or sulfone, the alkoxy, alkylthio and phenylthio being optionally substituted by one or more groups chosen from halogen, alkyl or alkoxy of 1 to 4 carbon atoms, trifluoromethyl, amino, mono or dialkylamino, cyano, phenyl, hydroxyl, free, salified or esterified carboxy, acyl and acyloxy.
  • the process as defined above is characterized in that a compound of the formula ##STR31## in which Hal is halogen reacted with an oxidizing agent to obtain a compound of the formula ##STR32## which is reacted with a compound of the formula ##STR33## in which R' 3 has the meaning indicated above to obtain a product of the formula ##STR34## in which R' 3 has the meaning indicated above which is reacted with a compound of the formula
  • R' 1 and Hal have the meaning above to obtain a product of the formula ##STR35## in which R' 1 and R' 3 have the meanings above, which either is subjected to an addition reaction on the CN, using a reagent capable of introducing R' 2 as defined above to obtain the product of the formula ##STR36## in which R' 1 , R' 2 and R' 3 have the meanings above which is optionally subjected to a substitution reaction of the oxygen of by a sulfur to obtain a product of the formula ##STR37## in which R' 1 , R' 2 and R' 3 have the meanings above, which optionally is converted into the a product of the formula ##STR38## in which R' 1 , R' 2 and R' 3 have the meanings .indicated above, which product of formula E 1 , L 1 or L 2 is subjected to a cyclization reaction in order to obtain a product of the formula ##STR39## in which R' 1 , R' 2 and R' 3 have the meanings above
  • a particular subject of the invention is the process as defined above for the preparation of products of formula I corresponding to 2-butyl-1-[[2'-carboxy-(1,1'-biphenyl)-4-yl]methyl]-4-(phenylthio)-1H-imidazole-5-carboxylic acid
  • a more particular subject of the invention is the process as defined above for the preparation of products of formula I corresponding to-ethyl 2-butyl-4-(methyl-thio)-1-[[2'-((((propylamino)-carbonyl)-amino)-sulfonyl)-(1,1'-biphenyl)-4-yl]-methyl]-1H-imidazole-5-carboxylate,
  • the product of formula B can be obtained by oxidation of the halide of formula A by means of hexamethylenetetramine in 50% acetic acid or N-oxide-N-methyl morpholine in a solvent such as dichloromethane, dichloroethane or toluene.
  • the product of formula A is such that Hal is preferably bromine but can also be chlorine or iodine.
  • the reaction of the compound of formula B with the compound of formula II can be carried out by a reducing amination, brought about in two stages:
  • the first stage is the formation of the imine of the product of formula B by the addition of the product of formula II on the aldehyde function of the product of formula B, in a solvent such as dichloromethane, dichloroethane or tetrahydrofuran preferably under acid catalysis conditions, for example in the presence of amberlyst H + or also acetic acid.
  • the second stage is the reduction of the imine formed by a reducing agent such as NaBH 3 CN or NaBH(OAc) 3 (prepared previously from sodium borohydride and acetic acid).
  • the product of formula C is converted into the product of formula D by an acylation agent, for example an acid halide such as butyryl or valeryl chloride in the presence of sodium or potassium carbonate, pyridine or triethylamine in a solvent such as acetone, tetrahydrofuran, dichloromethane or dichloroethane.
  • an acylation agent for example an acid halide such as butyryl or valeryl chloride in the presence of sodium or potassium carbonate, pyridine or triethylamine in a solvent such as acetone, tetrahydrofuran, dichloromethane or dichloroethane.
  • the product of formula D is converted into the product of formula E by the addition of R' 2 on the cyano function which amidification can take place in a solvent such as an alcohol like methanol or ethanol, by reaction of R' 2 --SH on the cyano function in a solvent such as toluene, tetrahydrofuran or dichloroethane.
  • reaction of the product of formula D to obtain the corresponding product of formula E is a thioamidification carried out by the action of a compound of formula R 10 --SH in which R 10 is the remainder of the R' 2 as defined above and notably alkyl of 1 to 4 carbon atoms or phenyl optionally substituted as indicated above.
  • the thioamidification can be carried out by bubbling the compound of formula R 10 --SH as defined above in a solvent such as an alcohol like ethanol or methanol or dichloroethane, dichloromethane, toluene, tetrahydrofuran in the presence of a base like triethylamine.
  • a solvent such as an alcohol like ethanol or methanol or dichloroethane, dichloromethane, toluene, tetrahydrofuran in the presence of a base like triethylamine.
  • the thioamidification can also be carried out with the R 10 SNa or R 10 SK reagent under the same solvent conditions defined for R 10 SH.
  • the substitution reaction of the oxygen by a sulfur to obtain the product of formula L can be carried out with Lawesson reagent.
  • the cyclization reaction of the product of formula E into the product of formula I' can be carried out either by an acid catalysis using amberlyst H + , tosylic acid or sulfuric acid in a solvent such as toluene, ethyl acetate, dichloromethane, dichloroethane, or with pentachloride in pyridine or dimethylaminopyridine, or also in dimethylsulfone.
  • the hydroxyl groups can be protected for example by alkyl such as tert-butyl, trimethylsilyl, tert-butyldimethylsilyl, methoxymethyl, tetrahydropyrannyl, benzyl or acetyl.
  • the amino groups can be protected for example by acetyl, trityl, benzyl, tertbutoxycarbonyl, phthalimido or by others known in the chemistry of the peptides.
  • Acyl groups such as formyl can be protected in the form of cyclic or non-cyclic ketals such as dimethyl- or diethylketal or ethylene dioxyketal and the acid functions of the products can be optionally amidified by a primary or secondary amine for example in methylene chloride in the presence of 1-ethyl-3-(dimethylaminopropyl)-carbodiimide hydrochloride at ambient temperature.
  • the acid functions can be protected for example in the form of esters formed with easily-cleavable esters such as benzyl or ter-butyl esters or esters known in the chemistry of the peptides.
  • the products of formulae D and E can be subjected during the process described above to the various reactions indicated above and notably reactions relating to R' 4 as defined above
  • the product of formula E 1 can be converted into product E 2 before continuing the synthesis as indicated above for the conversion of product D 1 into product D 2 .
  • ester functions into an acid function can optionally be carried out under the usual conditions known to one skilled in the art, notably by alkaline or acid hydrolysis for example with sodium hydroxide or potassium hydroxide in an alcoholic medium such as in methanol or with hydrochloric or sulfuric acid.
  • the optional cyano functions of the products can optionally be converted into an acid function under the usual conditions known to one skilled in the art, for example by a double hydrolysis carried out in an acid medium such as in a mixture of sulfuric acid, glacial acetic acid and water, these three compounds being preferably in equal proportions, or in a mixture of sodium hydroxide, ethanol and water at reflux.
  • an acid medium such as in a mixture of sulfuric acid, glacial acetic acid and water, these three compounds being preferably in equal proportions, or in a mixture of sodium hydroxide, ethanol and water at reflux.
  • the optional free or esterified carboxy functions of the products above can optionally be reduced into an alcohol function by methods known to one skilled in the art.
  • esterified carboxy functions lithium aluminum hydride can be used in a solvent such as tetrahydrofuran or dioxane or ethyl ether.
  • free carboxy functions boron hydride can preferred be used.
  • the optional alkoxy functions such as methoxy of the products can optionally be, converted into a hydroxyl function under the usual conditions known to one skilled in the art, for example by boron tribromide in a solvent such as methylene chloride, by pyridine hydrobromide or hydrochloride or by hydrobromic or hydrochloric acid in water or by acetic acid at reflux.
  • the optional groups containing a sulfur atom of the products can optionally be converted into a corresponding sulfoxide or sulfone function under the usual conditions known to one skilled in the art, such as by means of a peracid such as peracetic acid or metachloroperbenzoic acid or by ozone, oxone, sodium periodate in a solvent such as methylene chloride or dioxane at ambient temperature.
  • a peracid such as peracetic acid or metachloroperbenzoic acid
  • ozone oxone
  • sodium periodate sodium periodate in a solvent such as methylene chloride or dioxane at ambient temperature.
  • the sulfoxide function can be obtained by an equimolar mixture of the product containing an alkylthio or arylthio group and a reagent such as a peracid.
  • the sulfone function can be obtained by a mixture of the product containing an alkylthio or arylthio group with an excess of reagent such as a peracid.
  • the optional alcohol function of the products can optionally be converted into an aldehyde or acid function by oxidation under the usual conditions known to one skilled in the art such as by the action of manganese oxide to obtain the aldehydes or of Jones reagent to obtain the acids.
  • nitrile functions of the products can optionally be converted into tetrazole under the usual conditions known to one skilled in the art, such as by cycloaddition of a metal azide such as a trialkyltin azide on the nitrile function as indicated in the method described in the article, KOZIMA et al, J. Organometallic Chemistry, Vol. 33, p. 337 (1971)
  • the products of formula I' are in addition optionally subjected to the reactions indicated below.
  • the elimination of the protective groups under the usual conditions known to one skilled in the art, notably by an acid hydrolysis carried out with an acid such as hydrochloric, benzene sulfonic or p-toluene sulfonic acid, formic acid or trifluoroacetic acid or also by a catalytic hydrogenation.
  • the phthalimido group can be eliminated by hydrazine.
  • the salification is carried out by a mineral or organic acid according to the usual methods known to one skilled in the art.
  • the resolution of the racemics to obtain the optically active forms of the products of formula I is carried out by the usual methods known to one skilled in the art.
  • the products are endowed with antagonistic properties for the angiotensin II receptor and are inhibitors of the effects of angiotensin II, especially of the vasoconstrictive effect and also of the trophic effect at the level of the myocytes.
  • the products of formula I as well as their addition salts with pharmaceutically acceptable mineral or organic acids can be used particularly as medicaments in the treatment of arterial hypertension, cardiac insufficiencies, renal insufficiencies and in the prevention of post-angioplastic recurrence of stenoses. They can also be used in the treatment of certain gastro-intestinal, gynaecological disorders and especially for a relaxing effect at the level of the uterus, in the form of pharmaceutical compositions containing as active ingredient at least one of the medicaments as defined above.
  • compositions can be administered buccally, rectally, parenterally or locally as a topical application on the skin and mucous membranes.
  • compositions can be solid or liquid and can be presented in all the. pharmaceutical forms currently used in human medicine such as tablets, dragees, capsules, granules, suppositories, injectable preparations, ointments, creams, gels and aerosol preparations by the usual methods.
  • the active ingredient can be incorporated with the excipients usually employed in these pharmaceutical compositions such as talc, gum arabic, lactose, starch, magnesium stearate, cocoa butter, aqueous or non-aqueous vehicles, fatty substances of animal or vegetable origin, paraffin derivatives, glycols, various wetting, dispersing or emulsifying agents, preservatives.
  • the usual dose, variable according to the product used, the patient being treated and the illness in question, can be, for example, from 1 to 100 mg per day in an adult, by oral route.
  • the products of formula III are commercially-available products or can be easily prepared from the acid or an appropriate derivative.
  • an object of the invention are the new industrial products, namely the compounds of formulae B, C, D, D 1 , D 2 , E, E 1 , E 2 , L, L 1 and L 2 .
  • STAGE B preparation of ethyl-cyano-[[[2'-[[[(propylamino)-carbonyl]-amino]-sulfonyl]-(1,1'-biphenyl)-4-yl]-methyl]-(1-oxopentyl)-amino]-acetate
  • STAGE F 2-butyl-4-(methylthio)-1-[[2'-[[[(propylamino)-carbonyl]-amino]-sulfonyl]-(1,1'-biphenyl)-4-yl]-methyl]-1H-imidazole-5-carboxylic-acid di-potassium salt

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Publication number Priority date Publication date Assignee Title
US5811445A (en) * 1994-03-04 1998-09-22 Roussel Uclaf Method of preventing abnormal stimulation of AT1 and AT2 receptors
WO2000001674A1 (fr) * 1998-07-01 2000-01-13 Merck & Co., Inc. Procede de production d'imidazoles 1,5-disubstitues
US6335451B1 (en) 1997-01-22 2002-01-01 Hoechst Aktiengesellschaft Five-membered heterocycles having biphenylsulfonyl substitution, with sulfonylcyanamide side chain, compositions containing them, and methods of using them
US6369236B1 (en) 1998-07-18 2002-04-09 Aventis Pharma Deutschland Gmbh Imidazole derivatives with biphenylsulfonyl substitution method for preparing them and their use as a drug or diagnostic agent
US6372917B1 (en) 1998-07-18 2002-04-16 Aventis Pharma Deutschland Gmbh Biphenylsulfonyl-substituted imidazole derivatives, their preparation process, their use as a drug or diagnostic agent and drug containing them
US8236843B2 (en) 2008-09-02 2012-08-07 Elder Pharmaceuticals Ltd. Anti inflammatory compounds

Families Citing this family (3)

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AU1600297A (en) * 1996-02-15 1997-09-02 Novartis Ag Aryl derivatives
US6080870A (en) * 1996-04-03 2000-06-27 Merck & Co., Inc. Biaryl substituted imidazole compounds useful as farnesyl-protein transferase inhibitors
US6063930A (en) * 1996-04-03 2000-05-16 Merck & Co., Inc. Substituted imidazole compounds useful as farnesyl-protein transferase inhibitors

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0465368A1 (fr) * 1990-07-05 1992-01-08 Roussel Uclaf Nouveaux dérivés soufrés de l'imidazole, leur procédé de préparation, les nouveaux intermédiaires obtenus, leur application à titre de médicaments et les compositions pharmaceutiques les renfermant
EP0503162A1 (fr) * 1991-01-04 1992-09-16 Hoechst Aktiengesellschaft Dérivés d'azole, procédé de leur fabrication et leur application

Family Cites Families (6)

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Publication number Priority date Publication date Assignee Title
ATA937274A (de) * 1973-12-17 1978-02-15 Thomae Gmbh Dr K Verfahren zur herstellung neuer araliphatischer ketone
ATE134624T1 (de) * 1990-02-19 1996-03-15 Ciba Geigy Ag Acylverbindungen
IE910913A1 (en) * 1990-03-20 1991-09-25 Sanofi Sa N-substituted heterocyclic derivates, their preparation¹and pharmaceutical compositions containing them
IE920175A1 (en) * 1991-02-11 1992-08-12 Zeneca Ltd Nitrogen heterocycles
TW209213B (fr) * 1991-08-21 1993-07-11 Yamanouchi Pharma Co Ltd
EP0550313A1 (fr) * 1991-12-30 1993-07-07 Synthelabo Nouveaux dérivés de 2-(tétrazol-5-yl)-(1,1'-biphényle), leur préparation et leur utilisation comme intermédiaires de synthèse

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0465368A1 (fr) * 1990-07-05 1992-01-08 Roussel Uclaf Nouveaux dérivés soufrés de l'imidazole, leur procédé de préparation, les nouveaux intermédiaires obtenus, leur application à titre de médicaments et les compositions pharmaceutiques les renfermant
EP0503162A1 (fr) * 1991-01-04 1992-09-16 Hoechst Aktiengesellschaft Dérivés d'azole, procédé de leur fabrication et leur application

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5811445A (en) * 1994-03-04 1998-09-22 Roussel Uclaf Method of preventing abnormal stimulation of AT1 and AT2 receptors
US5977155A (en) * 1994-03-04 1999-11-02 Hoechst Marion Roussel Imidazole-5-carboxamides
US6335451B1 (en) 1997-01-22 2002-01-01 Hoechst Aktiengesellschaft Five-membered heterocycles having biphenylsulfonyl substitution, with sulfonylcyanamide side chain, compositions containing them, and methods of using them
US6486189B2 (en) 1997-01-22 2002-11-26 Hoechst Aktiengesellschaft Five-membered heterocycles having biphenylsulfonyl substitution, process for their preparation, their use as a medicament or diagnostic, and medicament comprising them
WO2000001674A1 (fr) * 1998-07-01 2000-01-13 Merck & Co., Inc. Procede de production d'imidazoles 1,5-disubstitues
US6369236B1 (en) 1998-07-18 2002-04-09 Aventis Pharma Deutschland Gmbh Imidazole derivatives with biphenylsulfonyl substitution method for preparing them and their use as a drug or diagnostic agent
US6372917B1 (en) 1998-07-18 2002-04-16 Aventis Pharma Deutschland Gmbh Biphenylsulfonyl-substituted imidazole derivatives, their preparation process, their use as a drug or diagnostic agent and drug containing them
AU764438B2 (en) * 1998-07-18 2003-08-21 Sanofi-Aventis Deutschland Gmbh Imidazole derivatives with biphenylsulfonyl substitution, method for preparing them and their use as a drug or diagnostic agent
US8236843B2 (en) 2008-09-02 2012-08-07 Elder Pharmaceuticals Ltd. Anti inflammatory compounds

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